Position Title: Clinical Data Manager Work Location: Maple Grove, MN 55311 Assignment Duration: 6 months (potential to extend highly likely) Work Arrangement: Onsite minimum 4 days/week Main Purpose of Role The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk-based quality management systems, as described in the risk assessment, data management plan, and site and central monitoring plans. As the customer-face of Data Review and its primary liaison with the therapy group, the Clinical Data Manager's therapy-specific knowledge ensures alignment to customer definitions of criticality, and informs review and analysis of study data. Main Responsibilities Clinical Data Manager will oversee 3-5 clinical trials from data management perspective, and together with assigned Coordinator, takes care of all related activities from CRF design, clinical data review and oversight, to trial closure related data activities. Identification of study specific risks to study conduct and human subject safety; analysis of risks; development and implementation of mitigation strategies. Review of study data to detect anticipated and unanticipated issues related to trial data completeness and quality. Facilitate multi-stakeholder discussions to review findings, evaluate impact and develop action plans for correction and continued monitoring. Conduct Central Monitoring activities, as described in Central Monitoring Plan. Direct all data cleaning activity related to assigned studies. Qualifications: Bachelors Degree: Biology, Health Sciences, Mathematics, Computer Science, or equivalent. Experience/Background: Minimum 3 years 3 years in clinical operations or healthcare related field. Top Skills Needed: Analytical and critical thinking skills along with related work experience, Data management/Analysis (not statistical analysis) with the relative previous past work experience. Education and work experience in project management, life sciences and/or technical field. Knowledge of data collection best practices for clinical trials. Knowledge of global clinical operations. Experience in consultative role, with Subject Matter Expertise, and effectively influencing a team decision to the desired outcome. Proficient at the identification of risks in a process, evaluation of likelihood and impact, and the development of effective mitigation and monitoring strategies that are imperfect yet meet the business need. Proficient in the translation of clinical trial requirements to the technical specifications required for effective data collection. Skilled at making inferences and connections based on limited information, clearly describing the knowns, unknowns, and alternative explanations. Intermediate project management skills; developing a multifaceted plan with complex dependencies and holding peers accountable to adherence to the plan while maintaining positive and collaborative relationships. Intermediate therapy specific knowledge of anatomy, physiology, pathophysiology, therapy and device. Licenses and Certifications None required; Certified Clinical Data Manager (CCDM) or equivalent nice to have. SPECTRAFORCE is an equal opportunity employer and does not discriminate against any employee or applicant for employment because of race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability or veteran status, or any other category protected by applicable federal, state, or local laws. Please contact Human Resources at nahr@spectraforce.com if you require reasonable accommodation.
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